Paper - The development of the adrenal gland in man
|Embryology - 29 May 2020 Expand to Translate|
|Google Translate - select your language from the list shown below (this will open a new external page)|
العربية | català | 中文 | 中國傳統的 | français | Deutsche | עִברִית | हिंदी | bahasa Indonesia | italiano | 日本語 | 한국어 | မြန်မာ | Pilipino | Polskie | português | ਪੰਜਾਬੀ ਦੇ | Română | русский | Español | Swahili | Svensk | ไทย | Türkçe | اردو | ייִדיש | Tiếng Việt These external translations are automated and may not be accurate. (More? About Translations)
|A personal message from Dr Mark Hill (May 2020)|
|contributors to the site. The good news is Embryology will remain online and I will continue my association with UNSW Australia. I look forward to updating and including the many exciting new discoveries in Embryology!|
Crowder RE. The development of the adrenal gland in man, with special reference to origin and ultimate location of cell types and evidence in favor of the "cell migration" theory. (1957) Contrib. Embryol., Carnegie Inst. Wash. 36, 193-210.
|Historic Disclaimer - information about historic embryology pages|
|Embryology History | Historic Embryology Papers)|
The Development Of The Adrenal Gland In Man, With Special Reference To Origin And Ultimate Location Of Cell Types And Evidence In Favor Of The “Cell Migration” Theory
by Roy E. Crowder
With 8 plates and 7 text figures.
- The ideas herein expressed are those of the author and do not reflect those of the United States Navy.
A voluminous literature has accumulated on the development of the adrenal gland. In 1902, Iosef \Viesel apologized for adding one more article. Others, including the present author, have not been so restrained.
In a study of the sources of certain of the adrenal hormones, a review of the literature on the embryology and histology of the gland was undertaken. In spite of the number of articles published on the subject, including extensive reviews (Parkes, I945; Lanman, 1953), there was no consecutive life history of the source and ultimate distribution of the various cell types found in the gland. and, therefore, it was not possible to associate the synthesis of the adrenal hormones with specific cell types.
The wealth of closely seriated, well preserved, and adequately stained material available in the Carnegie Embryological Collection, in Baltimore, Maryland, made a complete histologic and embryologic study possible.
The study was begun with the idea of determining the types of cells in the adrenal cortex. It was soon found that, to do this adequately, the whole embryologic history must be reviewed. The results of this undertaking are set forth herein. It is hoped not only that they will assist in an understanding of the sequence of events in the histogenesis of the adrenal cortex and clarify a few of the points of controversy, but also that the descriptions of cell types in the cortex may be of value in determining the oligoplasia or hypcrplasia of certain of these cell types in relation to many clinical entities.
The following terms are defined to clarify the presentation:
Fetal cortex: The fetal adrenal cortex is composed of the same cell types as the adrenal cortex of the adult human, but the proportions and arrangements differ.
Medullary cells: The cells of neural origin which take up a location in the central portion of the gland during development. The process of localization begins in the embryonic period and continues until childhood.
Cell types: Cell types in the cortex are differentiated by the structure of their nuclei; they are numbered according to the order of their appearance in the primordium, as C-I (fig. 38, pl. 8), C-II (fig. 39, pl. 8), and C-III (fig. 40, pl. 8). As will be made clear, three distinct cell types may be recognized in the development of the medulla; these cells, designated M-I, M-II, and M-III, are described beginning on page 202.
Celomic epithelial cells: The cells of the adrenal cortex which have their origin in the celomic epithelium. They are of two types: Type C-I (fig. 38, pl. 8), the first cells to enter the primordium, are large polyhedral cells, each of which contains a large round nucleus with little chromatin, a large round nucleolus, and a spherical, refractile inclusion. In a later stage, type C-III cells (Hg. 40, pl. 8) begin to emerge from the celomic epithelium, together with type C-I. Type C-III cells are smaller than type C-1, and each contains a smaller round nucleus which stains more deeply with hematoxylin. In the nucleus. there is a large amount of chromatin, which tends to aggregate into four to five major clumps and one or two globules or vacuoles.
Cells of mesonephric origin: These cells arise from Bowman's capsule of the mesoncphros. They are designated as type C-II cells (fig. 39, pl. 8), and are first seen streaming from the glomerular capsule across the ventral portion of the early primordium (figs. 14, 15, pl. 2). The type C-II cells and their successors form most of the adrenal capsule, and, during horizon xxiii, are diverted inward by the arteriolar capillaries. Thereafter, they are found in the cords of cells within the cortex. Their nucleus is round, and stains a little more deeply than does that of type C-I. The chromatin is distributed in fine strands in a spider-like manner just beneath the nuclear membranes, the nucleolus corresponding to the body of the spider. The center of the nucleus is occupied by one or more large globules or vacuoles.
Immigration and migration: The passage of cells from one region to another; the addition of cells by movement from an adjacent region. Ameboid movement is not implied.
Invasion: The entrance of cells after destruction or disruption of pre-existing tissue, and the assumption of position without rcference to former relations.
Staging of embryos: The dating of the embryos follows the horizons described and graphed by Streeter (1951). This method of seriation affords a much better concept of the progress of development than does measurement of the length. Frequently, the organogenesis of the adrenal gland was found to be in a much further advanced stage in an embryo with a shorter crown-rump length than in a longer one, particularly in the earlier stages when the dorsal curvature varies so remarkably among embryos in the same horizon. This ﬁnding speaks well for the method, since Streeter did not use the adrenal among his criteria for staging. The age in weeks is the estimated conception age. To obtain menstrual age, two weeks must be added. There are enough stages to pro- vicle a consecutive account of the organogenesis of the adrenal.
Materials and Methods
The following embryos of the Carnegie Collection were selected for the study of the embryonic and early fetal development of the adrenal gland.
(table to be formatted)
Crown-Rump Length (mm.)
836 . . . . . . 4.0 Trans. Exc. A1. coch. 7433 . . . . . . 5.2 Frontal Exc. (Stain - Haematoxylin Eosin) 8066 . . . . . . 5.3 Trans. Exc. (Stain - Haematoxylin Eosin) 8119 . . . . . . 5.3 Trans. Exc. (Stain - Haematoxylin Eosin) Homzo.-' xtv 3805 . . . . . . 5.9 Trans. Exc. (Stain - Haematoxylin Eosin)
6502 . . . . . . 6.7 Trans. Exc. (Stain - Haematoxylin Eosin)
7324 . . . . . . 6.6 Trans. Good (Stain - Haematoxylin Eosin)
7829 . . . . . . 7.0 Trans. Exc. (Stain - Haematoxylin Eosin)
7370 . . . . . . 7.2 Trans. Exc. (Stain - Haematoxylin Eosin)
8314 . . . . . . 8.2 Trans. Exc. Azan 1-lomzow xv 2. . . . . . 7.0 Trans. Good Al. carm. 721 . . . . . . 9.0 Trans. lixc.
3385 . . . . . . 8.3 Trans. Exc. (Stain - Haematoxylin Eosin) or G.
3441 . . . . .. 8.0 Sag. Exc. Al. coch.
3512 . . . . . . S 5 Trans. Exc. Al. coch.
6504 . . . . . . 7 5 Sag. Exc. A1. coch.
6508 . . . . . . 7.3 Trans. Good Al. coch. 6595. . . . , 3.0 Sag. Good I-1.-17.. 7199 . . . . . , 8.-'1 Frontal Good Al. coch. phloxine 7364 . . . . . 9 5 Frontal Poor 1-1.-17.. 8929 . . . . . , 6 3 Frontal Exc. Azan 8997 . . . . . . 9 0 Trans. Exc. Azan 9140 . . . . . . 7 0 Trans. Exc. Azan I-Ioruzox xvt
792 . . . . . . 8 0 Trans. Good A1. coch.
6511 . . . . . . 8 1 Sag. Good Al. coch. iron H.
6512 . . . . .. 70 Trans. Exc. A1. coch.
6517 . . . . . . 10 5 Trans. Exc. Al. coch.
7115 . . . . .. 9 7 Frontal Exc. H. and pltloxinc
7804 . . . . . . 9 5 Trans. Good (Stain - Haematoxylin Eosin)
7897 . . . . . . 12 2 Trans. Good (Stain - Haematoxylin Eosin)
8773 . . . . . . ll 0 Frontal Exc. Azan l-lot-:1zo.\' xvu 940 . . . . . . 14 0 Trans. Good (Stain - Haematoxylin Eosin) or G.
5893 . . . . . . 13 2 Trans. Good Al. coch.
6253 . . . . . . 1-10 Trans. Good (Stain - Haematoxylin Eosin)
6519 , . . . . . 10 3 Sag. Exc. Al. coch.
6520 . . . . . . 14 2 Trans. Exc. Al. coch.
6742 . . . . . . 11 0 Trans. Good I-1.-pltloxine
6758 . , . . . . 12 8 Trans. Good 1-1.-phloxine
8101 . . . . .. 13.0 Trans. Exc. (Stain - Haematoxylin Eosin)
811$ . . . . .. 12.6 Frontal Exc. (Stain - Haematoxylin Eosin)
8789 . . . . . . ll 7 Sag. Exc. Azan
3998 . . . . . . 11 0 Frontal Exc. Azan
-192 . . . , . . 16.3 Frontal Exc. Al. coch.
1909 . . . . . . 14.6 Frontal Good .'-\l. coch. or G.
4430 . . . . .. 14.0 Trans. Exc. A1. coch. or G.
6524 . . . . . . 11.7 Trans. Exc. A1. coch.
6525 . . . . .. 13.8 Sag. Exc. Al. coch.
6527 . . . . .. 14.4 Trans. Exc. Al. coch.
6528 . . . . .. 13.4 Frontal Exc. A1. coch.
7707 . . . . .. 14 5 Trans. F.xc. 1-1.—F.. phloxine
8172 . . . . . . 16 5 Trans. Exc. (Stain - Haematoxylin Eosin)
S312 . . . . .. 12.2 Trans. F..\:c. I-1.717..
9247 . . . . .. 15.0 Sag. Exc. Azan
4-105 . . . . . . 15 5 Trans. Good Coch. l\1allor_\-' 4501 . . . . .. 180 Trans. F..\'c. Coclt. or G. 5609. . 18 0 Frontal F..\:c. Al. coch.
6150 . . . . . . 17.0 Trans. Good
632-l . . . . .. 18.5 Sag. Good (Stain - Haematoxylin Eosin)
S092. . . . . . 16 3 Trans. lixc. I-1.-E. phlo.\;ine 9113 . . . . . . 18 5 Trans. Exc. Azan
Horizon xx 966.. . 23.0 Frontal F.xc. A1. coch.
5537. . . . .. 22.0 Trans. Fxc. Al. coch. 6202... . .. 21.0 Sag. F.xc. (Stain - Haematoxylin Eosin)
S226 . . . . .. 18.0 Sag. Exc. Azan
5.596. . 21.5 Sag. Good I-1.-Ii.
725-1.. . 22.5 Trans. Exc.
7392.. . 22.7 Trans. Exc. (Stain - Haematoxylin Eosin)
Z864. . 24 0 Frontal F.:~:c. (Stain - Haematoxylin Eosin)
S553 . _ . _ . , 22.0 Trans. Exc. (Stain - Haematoxylin Eosin)
1458. . . . . , 27.5 Sag. Exc. or G 430-1. . 25 0 Trans. Good (Stain - Haematoxylin Eosin)
4638. , . 23.4 Trans. Exc. Al. coch
6701 . . . 24.0 Frontal Poor I-I.-E.
6832. . 25.8 Frontal Exc. I-1..F_.
339-1. . . 25 3 Trans. lixc. I1.-I’.
4205. . . . . . 29.5 Trans. Good Al coch
No. 4289. . . . . . 32.2 Trans. Good Al coch
4570 . . . . .. 30.7 Trans. Exc. (Stain - Haematoxylin Eosin)
5-122. . . . . . 27.0 Sag. Good (Stain - Haematoxylin Eosin)
5621.-\ . . . . 27.5 Trans. Good
6573. . . . . . 31.5 Trans. Good (Stain - Haematoxylin Eosin)
6719 . . . . .. 30.1 Trans. Good Chrom.alum hem. 7425 . . . . .. 27.0 Frontal Exc. Cl1I‘0111.:1lUI11l1CI]'l. 9226. . . . . . 30.1 Trans. Exc. Azan
Cite this page: Hill, M.A. (2020, May 29) Embryology Paper - The development of the adrenal gland in man. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Paper_-_The_development_of_the_adrenal_gland_in_man
- © Dr Mark Hill 2020, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G